HIGD1A antibody (Biotin)

Catalog No. ABIN1400641

This Rabbit Polyclonal antibody specifically detects HIGD1A in IHC (p). It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for HIGD1A antibody (Biotin) (ABIN1400641)

Target: HIGD1A (HIG1 Hypoxia Inducible Domain Family, Member 1A (HIGD1A))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HIGD1A antibody is conjugated to Biotin

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-HIGD1A Antibody (Biotin)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HIG1/HIGD1A

Isotype: IgG

Application Details

Application Notes: IHC-P 1:200-400

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for HIGD1A

Target: HIGD1A (HIG1 Hypoxia Inducible Domain Family, Member 1A (HIGD1A))

Alternative Name: HIG1

Background:

Synonyms: Hig1, HIG1 domain family member 1A, HIG1 domain family, member 1A, HIG1 hypoxia inducible domain family, member 1A, HIG1A_HUMAN, HIGD1A, HIMP1, Hypoxia-inducible gene 1 protein.

Background: HIGD1A (HIG1 domain family member 1A), also known as HIG1 (hypoxia-inducible gene 1 protein) or HSPC010, is a 93 amino acid multi-pass membrane protein that contains one HIG1 domain. Existing as two alternatively spliced isoforms, the gene encoding HIGD1A maps to human chromosome 3, which contains approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene ID: 25994